WO2002072747A1 - Bleaching catalysts with unsaturated surfactant and antioxidant - Google Patents

Bleaching catalysts with unsaturated surfactant and antioxidant Download PDF

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Publication number
WO2002072747A1
WO2002072747A1 PCT/EP2002/002768 EP0202768W WO02072747A1 WO 2002072747 A1 WO2002072747 A1 WO 2002072747A1 EP 0202768 W EP0202768 W EP 0202768W WO 02072747 A1 WO02072747 A1 WO 02072747A1
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WIPO (PCT)
Prior art keywords
bleaching
surfactant
bleaching composition
composition according
present
Prior art date
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PCT/EP2002/002768
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English (en)
French (fr)
Inventor
Ronald Hage
Roelant Mathijs Hermant
Jean Hypolites Koek
Simon Marinus Veerman
Original Assignee
Unilever Plc
Unilever Nv
Hindustan Lever Limited
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Application filed by Unilever Plc, Unilever Nv, Hindustan Lever Limited filed Critical Unilever Plc
Priority to BRPI0206044-2B1A priority Critical patent/BR0206044B1/pt
Priority to EP02732479A priority patent/EP1368451B1/en
Priority to AU2002304851A priority patent/AU2002304851B2/en
Priority to CA2431006A priority patent/CA2431006C/en
Priority to DE60220381T priority patent/DE60220381T2/de
Publication of WO2002072747A1 publication Critical patent/WO2002072747A1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/0084—Antioxidants; Free-radical scavengers
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/26—Organic compounds containing nitrogen
    • C11D3/28—Heterocyclic compounds containing nitrogen in the ring
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39—Organic or inorganic per-compounds
    • C11D3/3902—Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905—Bleach activators or bleach catalysts
    • C11D3/3932—Inorganic compounds or complexes

Definitions

  • This invention relates to the protection of an unsaturated surfactant in a bleaching composition.
  • UK patent application 0030877.5 filed 18-Dec-2000, discloses the use of an unsaturated surfactant as a bleach enhancement catalyst.
  • an unsaturated surfactant as a bleach enhancement catalyst.
  • stability problems associated with the interaction of the unsaturated surfactant and bleach enhancement catalyst .
  • the present invention provides a bleaching composition comprising an organic ligand which forms a complex with a transition metal for bleaching a substrate with a group selected from:
  • the bleaching composition upon addition to an aqueous medium providing an aqueous bleaching medium substantially devoid of a peroxygen bleach or a peroxy-based or peroxyl -generating bleach system; and, b) a peroxygen bleach or source thereof,
  • a bleaching composition for bleaching a substrate comprising:
  • the bleaching composition is substantially devoid of a peroxygen bleach or a peroxy-based or peroxyl -generating bleach system. Nevertheless, as another aspect of the present invention a peroxyl source may be present such that "air bleaching" is suppressed. Generally, "air bleaching" catalysts are capable of operating in a peroxyl bleaching mode.
  • the surfactant having an allylic hydrogen has an HLB (hydrophilic/lipophilic balance) greater that 2, more preferably greater than 5, and most preferably greater than 10. Ideally, if the surfactant is a charged species the HLB is greater than 15.
  • HLB hydrophilic/lipophilic balance
  • the HLB value requirement reflects the importance of the rate of solubility and dispersibility of the surfactant having an allylic hydrogen from the bleaching composition to the aqueous wash medium in conjunction with surface activity towards the substrate being washed.
  • the threshold value of HLB as required excludes compounds that have an allylic which do not have the required surfactant properties, for example linoleaic or oleic acid have an HLB of 0.8.
  • the surfactant having an allylic hydrogen has a CMC of 2 x 10 "2 M or less. It is most preferred that the surfactant is anionic has a critical micelle concentration value of 3 x 10 "3 M or less.
  • a surfactant will form a micelle when present in an aqueous solution above a specific concentration that is intrinsic to the surfactant.
  • a micelle is a neutral or electrically charged colloidal particle, consisting of oriented molecules.
  • CMC amphiphilic compounds tend to adopt specific aggregates in aqueous solution. The tendency is to avoid contact between their hydrophobic alkyl chains and the aqueous environment and to form an internal hydrophobic phase.
  • Such compounds can form monomolecular layers [monolayers] at the air-water boundary and bimolecular layers [bilayers] between two aqueous compartments.
  • Micelles are spherically closed monolayers. This CMC criterion is another aspect that aids reduction of catalyst deposit.
  • the surfactant used in the present invention is and forms a micelle at a concentration of 2 x 10 "2 M and below in an aqueous solution at a temperature of 25°C.
  • the standard CMC is measured in deionized water and that the presence of other components in solution, e.g. surfactants or ions in solution will perturb the CMC value.
  • the CMC values and requirement thereof as described herein are measured under standard conditions (N. M. Van Os, J. R. Haak, and L. A. M Rupert, Pysico Chemical Properties of Selected Anionic Cationic and Nonionic Surfactants Elsevier 1993; Kresheck, G. C.
  • the present invention has particular utility as a bleaching composition in a commercial "air bleaching" liquid and granular “air bleaching” or peroxyl bleaching format.
  • the degradation of unsaturated components during storage in the absence of an antioxidant often results in the formation of mal odour components due to the degradation of unsaturated compounds.
  • the composition also serves to reduce the degradation of unsaturated compounds during the wash.
  • composition of the present invention in an air bleaching mode, is preferably substantially devoid of a peroxygen bleach or a peroxy-based or peroxyl -generating bleach system.
  • the term "substantially devoid of a peroxygen bleach or a peroxy-based or peroxyl -generating bleach system" should be construed within spirit of the invention. It is preferred that the composition has as low a content of a peroxyl species present as possible. Nevertheless, autoxidation is something that is very difficult to avoid and as a result small levels of peroxyl species may be present. These small levels may be as high as 2% but are preferably below 2%.
  • the level of peroxide present is expressed in mMol of hydroperoxide (-OOH) present per Kg.
  • the additionally added organic compounds having labile CH's are particularly susceptible to autoxidation and hence may contribute more to this level of peroxyl species than other components.
  • an antioxidant in the composition will likely serve to reduce the presence of adventitious peroxyl species by reducing chain reactions.
  • the composition of the present invention bleaches a substrate with at least 10 %, preferably at least 50 % and optimally at least 90 % of any bleaching of the substrate being effected by oxygen sourced from the air.
  • total peroxyl present [RC (O) OOH] + [RC(0)00 " ].
  • total peroxyl present [RC(0)OOH] + [RC(0)0Cf] + [H 2 0 2 ] + [HOCT] .
  • the peroxy species will be relatively unreactive and hence the dominant conditions for "air bleaching" will be still be met by a relatively high level of peroxyl species present.
  • the present invention extends to a commercial package comprising the bleaching composition according to the present invention together with instructions for its use.
  • Any suitable textile that is susceptible to bleaching or one that one might wish to subject to bleaching may be used.
  • the textile is a laundry fabric or garment.
  • the method according to the present invention is carried out on a laundry fabric using an aqueous treatment liquor.
  • the treatment may be effected in a wash cycle for cleaning laundry. More preferably, the treatment is carried out in an aqueous detergent bleach wash liquid, preferably in a washing machine .
  • composition of the present invention whilst providing an improved amount protection to unsaturated compounds permits a bleaching activity of at least 25 %, preferably at least 50 %, equivalent to same composition devoid of antioxidant.
  • a unit dose as used herein is a particular amount of the bleaching composition used for a type of wash.
  • the unit dose may be in the form of a defined volume of powder, granules or tablet or unit dose detergent liquid.
  • compositions of the present invention will comprise an effective amount of the anti-oxidant, preferably from about 0.001 % more preferably from about 0.1%, most preferably from about 0.2% to about 10%, preferably to about 5%, more preferably to about 1% by weight of an anti-oxidant.
  • Anti- oxidants are substances as described in Kirk-Othmers (Vol 3, pg 424) and in Uhlmans Encyclopedia (Vol 3, pg 91) .
  • alkylated phenols having the general formula:
  • R wherein R is C1-C22 linear or branched alkyl, preferably methyl or branched C3-C6 alkyl; C3-C6 alkoxy, preferably methoxy; Rl is a C3-C6 branched alkyl, preferably tert- butyl ; x is 1 or 2.
  • Hindered phenolic compounds are preferred as antioxidant.
  • Another class of anti-oxidants suitable for use in the present invention is a benzofuran or benzopyran derivative having the formula:
  • Rl and R2 are each independently alkyl or Rl and R2 can be taken together to form a C5-C6 cyclic hydrocarbyl moiety;
  • B is absent or CH2 ;
  • R4 is C1-C6 alkyl;
  • R5 is hydrogen or -C(0)R3 wherein R3 is hydrogen or C1-C19 alkyl;
  • R6 is C1-C6 alkyl;
  • R7 is hydrogen or C1-C6 alkyl;
  • X is - CH20H, or - CH2A wherein A is a nitrogen comprising unit, phenyl, or substituted phenyl.
  • Preferred nitrogen comprising A units include amino, pyrrolidino, piperidino, morpholino, piperazino, and mixtures thereof.
  • antioxidants are found as follows.
  • Anti-oxidants/radical scavengers such as ascorbic acid (vitamin C) and its salts, tocopherol (vitamin E) , tocopherol sorbate, other esters of tocopherol, butylated hydroxy benzoic acids and their salts, gallic acid and its alkyl esters, especially propyl gallate, uric acid and its salts and alkyl esters, sorbic acid and its salts, the ascorbyl esters of fatty acids, amines (e.g., N,N-diethylhydroxylamine, amino-guanidine) , sulfhydryl compounds (e.g., glutathione) , and dihydroxy fumaric acid and its salts may be used.
  • amines
  • Non-limiting examples of anti-oxidants suitable for use in the present invention include phenols inter alia 2,6-di- tert-butylphenol, 2 , 6-di-tert-butyl-4-methylphenol , mixtures of 2 and 3- tert-butyl-4-methoxyphenol , and other ingredients including include propyl gallate, tert- butylhydroquinone, benzoic acid derivatives such as methoxy benzoic acid, methylbenzoic acid, dichloro benzoic acid, dimethyl benzoic acid, 5-hydroxy-2 , 2 , 4 , 6, 7- pentamethyl-2 , 3-dihydro-l-benzofuran-3 -one, 5-hydroxy-3- methylene-2 ,2,4,6, 7 -pentamethyl-2 , 3-dihydro-benzofuran, 5- benzyloxy-3-hydroxymethyl-2, 2,4,6, 7 -pentamethyl-2 , 3-dihydro- l-benzofuran, 3-hydroxymethyl
  • Preferred radical scavengers for use herein include di-tert- butyl hydroxy toluene (BHT) , ⁇ -tocopherol .
  • hydroquinone 2,2, 4-trimethyl-l, 2-dihydroquinoline, di-tert -butyl hydroquinone, mono-tert -butyl hydroquinone, tert-butyl - hydroxy anisole, benzoic acid and derivatives thereof, like alkoxylated benzoic acids, as for example, trimethoxy benzoic acid (TMBA) , toluic acid, catechol , t-butyl catechol, benzylamine, 1 , 1 , 3-tris (2-methyl-4-hydroxy-5-t- butylphenyl) butane, N-propyl -gallate or mixtures thereof and highly preferred is di-tert-butyl hydroxy toluene.
  • TMBA trimethoxy benzoic acid
  • TMBA trimeth
  • the surfactant having an allylic hydrogen is present in the composition such that a unit dose provides at least 0.01 g/1, more preferably at least 0.5g /l, and most preferably at least 0. lg /l, concentration of the unsaturated organic compound in a wash.
  • the surfactant having an allylic hydrogen may be present in the composition in the range of 0.01 to 60%, preferably 0.1 to 20% and most preferably 10% w/w.
  • surfactants having an allylic hydrogen there are many classes of surfactants having an allylic hydrogen that will work with the present invention to enhance air bleaching.
  • a surfactant having an allylic hydrogen may be found in: neutral species, and charged species, i.e., cationic species, anionic species, and zwitterionic species. It is preferred that the surfactant having an allylic hydrogen contains a hydrophilic group thereby providing the organic compound unassociated or as a micelle in an aqueous medium. It also is preferred that the surfactant having an allylic hydrogen is provided in the form of an alkali metal salt, preferably sodium, of an unsaturated carboxylic acid.
  • the homolytic bond dissociation energy (BDE) for benzene (C6H5-H) is 110.9 kcal/mol (298 K) makes benzene moieties per se unsuitable to promote enhanced bleaching.
  • the surfactant having an allylic hydrogen has a molecular weight of at least 80 and a bond dissociation energy of less than 95 kcal/mol, most preferably below 90 kcal/mol, and even more preferably below 85 kcal/mol.
  • bond strengths (298 K) obtained from: The handbook of Chemistry and Physics 73 rd edition, CRC Press.
  • Unsaturated Soap Unsaturated Anionic Surfactant
  • the unsaturated fatty acid soap used preferably contains from about 16 to about 22 carbon atoms, preferably in a straight chain configuration. Preferably the number of carbon atoms in the unsaturated fatty acid soap is from about 16 to about 18.
  • This unsaturated soap in common with other anionic detergents and other anionic materials in the detergent compositions of this invention, has a cation, which renders the soap water-soluble and/or dispersible.
  • Suitable cations include sodium, potassium, ammonium, monethanolammonium, diethanolammonium, triethanolammonium, tetramethylammonium, etc. cations.
  • Sodium ions are preferred although in liquid formulations potassium, monoethanolammonium, diethanolammonium, and triethanolammonium cations are useful .
  • the unsaturated soaps are made from natural oils that often contain one or more unsaturated groups and consist of mixtures of components. It is clear that hydrolysation of these natural components yield mixtures of soaps, of which at least one of the components contain one or more unsaturated groups.
  • natural oils are sunflower oil, olive oil, cottonseed oil, linseed oil, safflower oil, sesame oil, palm oil, corn oil, peanut oil, soybean oil, castor oil, coconut oil, canola oil, cod liver oil and the like, that give mixtures of soaps of which at least one of them has at least one unsaturated group.
  • hydrolysis products of purified oils, as listed above may be employed.
  • Other examples of soaps include thoses derived from erucic acid,
  • Unsaturated Surfactant (Unsaturated Cationic)
  • unsaturated cationic may be manufactured, for example, by adding an unsaturated alkyl halide to an amine thus forming an unsaturated cationic.
  • cationic surfactants exhibit the same requirements as listed above for the unsaturated soap materials, except they need to be quarternised.
  • suitable cationics may be formed by preparing the quaternary salts from alcohols that were obtained from the corresponding fatty acid (as defined under 1; from oils containing unsaturated bonds) .
  • cationic surfactants based on natural oils include oleylbis (2-hydroxyethyl) methylammonium chloride and ditallow fatty alkyldimethyl ammonium chloride.
  • non- ionic (neutral) surfactant is found in alkoxylated non- ionic surfactants.
  • the surfactant has an allylic hydrogen .
  • the bleach catalyst per se may be selected from a wide range of organic molecules (ligands) and complexes thereof. Suitable organic molecules (ligands) and complexes for use with the present invention are found, for example in:
  • an air bleaching catalyst is a ligand or transition metal catalyst thereof of a ligand having the formula (I) : Rl
  • each R is independently selected from: hydrogen, hydroxyl, and CI -C4 -alkyl ;
  • Rl and R2 are independently selected from: Cl-C4-alkyl, C6-CIO -aryl, and, a group containing a heteroatom capable of coordinating to a transition metal, wherein at least one of Rl and R2 is the group containing the heteroatom;
  • R3 and R4 are independently selected from hydrogen, C1-C8 alkyl, Cl-C8-alkyl-0-Cl-C8-alkyl, Cl-C8-alkyl-O-C6-C10-aryl, C6-C10-aryl, Cl-C8-hydroxyalkyl , and - (CH2) n C (0) OR5 wherein R5 is Cl-C4-alkyl, n is from 0 to 4 , and mixtures thereof; and,
  • the group containing the hetroatom is: a heterocycloalkyl : selected from the group consisting of: pyrrolinyl; pyrrolidinyl ; morpholinyl ; piperidinyl; piperazinyl ; hexamethylene imine; 1 , 4-piperazinyl ; tetrahydrothiophenyl ; tetrahydrofuranyl ; tetrahydropyranyl ; and oxazolidinyl , wherein the heterocycloalkyl may be connected to the ligand via any atom in the ring of the selected heterocycloalkyl, a -Cl-C6-alkyl-heterocycloalkyl , wherein the heterocycloalkyl of the -Cl-C6-heterocycloalkyl is selected from the group consisting of: piperidinyl ; piperidine; 1,4- piperazine, tetrahydrothioph
  • Cl-C6-alkylheteroaryl is selected from the group consisting of: pyridinyl; pyrimidinyl ; pyrazinyl; triazolyl; pyridazinyl ; 1 , 3 , 5-triazinyl ; quinolinyl; isoquinolinyl ; quinoxalinyl ; imidazolyl; pyrazolyl; benzimidazolyl; thiazolyl; oxazolidinyl; pyrrolyl; carbazolyl; indolyl ; and isoindolyl, wherein the heteroaryl may be connected to the -
  • Cl-C6-alkyl via any atom in the ring of the selected heteroaryl and the selected heteroaryl is optionally substituted by -Cl-C4-alkyl, a C0-C6-alkyl-phenol or thiophenol, a C2-C4-alkyl-thiol, thioether or alcohol, a C2-C4-alkyl-amine, and a C2-C4 -alkyl -carboxylate.
  • the ligand forms a complex with one or more transition metals, in the latter case for example as a dinuclear complex.
  • Suitable transition metals include for example: manganese in oxidation states II-V, iron II-V, copper I-III, cobalt I-III, titanium II-IV, tungsten IV-VI , vanadium II-V and molybdenum II -VI.
  • the transition metal complex preferably is of the general formula (Al) :
  • M represents a metal selected from Mn (II) - (III) - (IV) - (V), Cu(I)-(II)-(III) , Fe (II) - (III) - (IV) - (V) , Co(I)-(II)- (III), Ti(II) - (III) - (IV) , V(II) - (III) - (IV)-(V) , ModU- (III) - (IV) - (V) - (VI) and W(IV) - (V) - (VI) , preferably from Fe(II)-(III)-(IV)-(V) ;
  • L represents the ligand, preferably N,N-bis (pyridin-2- yl -methyl) -1, 1-bis (pyridin-2-yl) -1-aminoethane, or its protonated or deprotonated analogue;
  • X represents a coordinating species selected from any mono, bi or tri charged anions and any neutral molecules able to coordinate the metal in a mono, bi or tridentate manner;
  • the organic molecule (ligand) or transition metal complex is present in the composition such that a unit dose provides at least 0.1 ⁇ M of the organic molecule or transition metal complex thereof.
  • the present invention may be used in a peroxyl bleaching mode in contrast to an air bleaching mode in which the composition is substantially devoid of a peroxyl source. However it is preferred to use the present invention in an air bleaching mode. In this instance a purely peroxyl bleaching catalyst may be employed in contrast to an air bleaching catalyst.
  • the composition of the present invention uses a peroxyl species to bleach a substrate.
  • the peroxy bleaching species may be a compound which is capable of yielding hydrogen peroxide in aqueous solution.
  • Hydrogen peroxide sources are well known in the art. They include the alkali metal peroxides, organic peroxides such as urea peroxide, and inorganic persalts, such as the alkali metal perborates, percarbonates, perphosphates persilicates and persulphates . Mixtures of two or more such compounds may also be suitable.
  • sodium perborate tetrahydrate and, especially, sodium perborate monohydrate are particularly preferred.
  • Sodium perborate monohydrate is preferred because of its high active oxygen content.
  • Sodium percarbonate may also be preferred for environmental reasons.
  • the amount thereof in the composition of the invention usually will be within the range of about 1-35% by weight, preferably from 5-25% by weight.
  • a bleach precursor e.g., N,N,N'N' -tetraacetyl ethylene diamine (TAED) .
  • TAED N,N,N'N' -tetraacetyl ethylene diamine
  • Another suitable hydrogen peroxide generating system is a combination of a C1-C4 alkanol oxidase and a C1-C4 alkanol, especially a combination of methanol oxidase (MOX) and ethanol .
  • MOX methanol oxidase
  • Such combinations are disclosed in International Application PCT/EP 94/03003 (Unilever) , which is incorporated herein by reference.
  • Alkylhydroxy peroxides are another class of peroxy bleaching compounds. Examples of these materials include cumene hydroperoxide and t -butyl hydroperoxide .
  • Organic peroxyacids may also be suitable as the peroxy bleaching compound.
  • Such materials normally have the general formula :
  • R is an alkylene or substituted alkylene group containing from 1 to about 20 carbon atoms, optionally having an internal amide linkage; or a phenylene or substituted phenylene group; and Y is hydrogen, halogen, alkyl, aryl, an imido-aromatic or non-aromatic group, a COOH or
  • Typical monoperoxy acids useful herein include, for example
  • peroxybenzoic acid and ring-substituted peroxybenzoic acids e.g. peroxy- . alpha . -naphthoic acid
  • aliphatic, substituted aliphatic and arylalkyl monoperoxyacids e.g. peroxylauric acid, peroxystearic acid and N,N-phthaloylaminoperoxy caproic acid (PAP)
  • PAP N,N-phthaloylaminoperoxy caproic acid
  • Typical diperoxyacids useful herein include, for example:
  • inorganic peroxyacid compounds are suitable, such as for example potassium monopersulphate (MPS) . If organic or inorganic peroxyacids are used as the peroxygen compound, the amount thereof will normally be within the range of about 2-10% by weight, preferably from 4-8% by weight.
  • Peroxyacid bleach precursors are known and amply described in literature, such as in the British Patents 836988; 864,798; 907,356; 1,003,310 and 1,519,351; German Patent 3,337,921; EP-A-0185522 ; EP-A-0174132 ; EP-A- 0120591 ; and U.S. Pat. Nos.
  • peroxyacid bleach precursors are those of the cationic i.e. quaternary ammonium substituted peroxyacid precursors as disclosed in US Pat. Nos. 4,751,015 and 4,397,757, in EP-A0284292 and EP-A-331 , 229.
  • peroxyacid bleach precursors of this class are:
  • ODC N-octyl-N,N-dimethyl-NlO-carbophenoxy decyl ammonium chloride
  • a further special class of bleach precursors is formed by the cationic nitriles as disclosed in EP-A-303,520 and in European Patent Specification No.'s 458,396 and 464,880.
  • peroxyacid bleach precursors can be used in the present invention, though some may be more preferred than others .
  • the preferred classes are the esters, including acyl phenol sulphonates and acyl alkyl phenol sulphonates; the acyl-amides; and the quaternary ammonium substituted peroxyacid precursors including the cationic nitriles.
  • Examples of said preferred peroxyacid bleach precursors or activators are sodium-4-benzoyloxy benzene sulphonate (SBOBS) ; N,N,N'N' -tetraacetyl ethylene diamine (TAED) ; sodium- 1-methyl-2 -benzoyloxy benzene-4 -sulphonate; sodium-4- methyl-3-benzoloxy benzoate; SPCC; trimethyl ammonium toluyloxy-benzene sulphonate; sodium nonanoyloxybenzene sulphonate (SNOBS); sodium 3 , 5 , 5-trimethyl hexanoyl- oxybenzene sulphonate (STHOBS) ; and the substituted cationic nitriles .
  • SBOBS sodium-4-benzoyloxy benzene sulphonate
  • TAED N,N,N'N' -tetraacetyl ethylene diamine
  • TAED sodium- 1-
  • bleach precursors for use with the present invention are found in WO0015750, for example 6- (nonanamidocaproyl ) oxybenzene sulphonate .
  • the precursors may be used in an amount of up to 12%, preferably from 2-10% by weight, of the composition.
  • the Detergent Composition is a composition.
  • the air bleach catalyst and unsaturated organic compound may be used in a detergent composition specifically suited for stain bleaching purposes, and this constitutes a second aspect of the invention.
  • the composition comprises a surfactant and optionally other conventional detergent ingredients.
  • the invention in its second aspect provides an enzymatic detergent composition which comprises from 0.1 - 50 % by weight, based on the total detergent composition, of one or more surfactants.
  • This surfactant system may in turn comprise 0 - 95 % by weight of one or more anionic surfactants and 5 to 100 % by weight of one or more nonionic surfactants.
  • the surfactant system may additionally contain amphoteric or zwitterionic detergent compounds, but this in not normally desired owing to their relatively high cost.
  • the enzymatic detergent composition according to the invention will generally be used as a dilution in water of about 0.05 to 2%.
  • nonionic and anionic surfactants of the surfactant system may be chosen from the surfactants described "Surface Active Agents” Vol. 1, by Schwartz & Perry, Interscience 1949, Vol. 2 by Schwartz, Perry & Berch, Interscience 1958, in the current edition of "McCutcheon's Emulsifiers and Detergents” published by Manufacturing Confectioners Company or in "Tenside-Taschenbuch” , H. Stache, 2nd Edn. , Carl Hauser Verlag, 1981.
  • Suitable nonionic detergent compounds which may be used include, in particular, the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide either alone or with propylene oxide.
  • Specific nonionic detergent compounds are C 6 -C 22 alkyl phenol -ethylene oxide condensates, generally 5 to 25 EO, i.e. 5 to 25 units of ethylene oxide per molecule, and the condensation products of aliphatic C 8 - Ci ⁇ primary or secondary linear or branched alcohols with ethylene oxide, generally 5 to 40 EO.
  • Suitable anionic detergent compounds which may be used are usually water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.
  • suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher C 8 -C ⁇ 8 alcohols, produced for example from tallow or coconut oil, sodium and potassium alkyl C 9 -C 20 benzene sulphonates, particularly sodium linear secondary alkyl C ⁇ 0 -C ⁇ 5 benzene sulphonates; and sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum.
  • the preferred anionic detergent compounds are sodium Cn-C ⁇ 5 alkyl benzene sulphonates and sodium C ⁇ 2 -C ⁇ 8 alkyl sulphates.
  • surfactants such as those described in EP-A-328 177 (Unilever) , which show resistance to salting-out, the alkyl polyglycoside surfactants described in EP-A-070 074, and alkyl monoglycosides .
  • Preferred surfactant systems are mixtures of anionic with nonionic detergent active materials, in particular the groups and examples of anionic and nonionic surfactants pointed out in EP-A-346 995 (Unilever) .
  • surfactant system that is a mixture of an alkali metal salt of a C 16 -Ci 8 primary alcohol sulphate together with a C 12 -C 15 primary alcohol 3-7 EO ethoxylate .
  • the nonionic detergent is preferably present in amounts greater than 10%, e.g. 25-90% by weight of the surfactant system.
  • Anionic surfactants can be present for example in amounts in the range from about 5% to about 40% by weight of the surfactant system.
  • the detergent composition may take any suitable physical form, such as a powder, granular composition, tablets, a paste or an anhydrous gel .
  • the detergent compositions of the present invention may additionally comprise one or more enzymes, which provide cleaning performance, fabric care and/or sanitation benefits .
  • Said enzymes include oxidoreductases, transferases, hydrolases, lyases, isomerases and ligases. Suitable members of these enzyme classes are described in Enzyme nomenclature 1992: recommendations of the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology on the nomenclature and classification of enzymes, 1992, ISBN 0-12-227165-3, Academic Press.
  • composition may contain additional enzymes as found in WO 01/00768 Al page 15, line 25 to pagel9, line 29, the contents of which are herein incorporated by reference.
  • Builders, polymers and other enzymes as optional ingredients may also be present as found in WO0060045.
  • Suitable detergency builders as optional ingredients may also be present as found in WO0034427.
  • composition of the present invention may be used for laundry cleaning, hard surface cleaning (including cleaning of lavatories, kitchen work surfaces, floors, mechanical ware washing etc.) .
  • bleaching compositions are also employed in waste-water treatment, pulp bleaching during the manufacture of paper, leather manufacture, dye transfer inhibition, food processing, starch bleaching, sterilisation, whitening in oral hygiene preparations and/or contact lens disinfection.
  • bleaching should be understood as relating generally to the decolourisation of stains or of other materials attached to or associated with a substrate.
  • the present invention can be applied where a requirement is the removal and/or neutralisation by an oxidative bleaching reaction of malodours or other undesirable components attached to or otherwise associated with a substrate.
  • bleaching is to be understood as being restricted to any bleaching mechanism or process that does not require the presence of light or activation by light.
  • the ligand N,N-bis (pyridin- 2-yl-methyl) -1 , 1-bis (pyridin-2- yl) -1-aminoethane (MeN4py) was prepared as described in EP 0 909 809 A2.
  • the ligand MeN4Py (33.7 g; 88.5mmoles) was dissolved in 500ml dry methanol. Small portions of FeCl 2 .4H 2 0 (0.95 eq; 16.7 g; 84.0 mmoles) were added, yielding a clear red solution. After addition, the solution was stirred for 30 minutes at room temperature, after which the methanol was removed (rotary-evaporator) .
  • Liquid formulation A was prepared with 0.03% of
  • the anti-oxidants employed were: BHT (2 , 6-di-t-butyl-4- methylphenol) , Trolox (6-hydroxy-2 , 5 , 7, 8-tetramethylchroman- 2-carboxylic acid, Raluquin (1 , 2-dihydro-6-ethoxy-2 , 2 , 4- trimethylchinolin, vitamin C, Vitamin E ( ⁇ -tocopherol) , vitamin E-acetate (O-acetyl- ⁇ -tocopherol) , and a mixture of 10% ⁇ , 45% ⁇ - and 45% ⁇ -tocopherol .
  • BHT 6-di-t-butyl-4- methylphenol
  • Trolox 6-hydroxy-2 , 5 , 7, 8-tetramethylchroman- 2-carboxylic acid
  • Raluquin (1 , 2-dihydro-6-ethoxy-2 , 2 , 4- trimethylchinolin
  • vitamin C Vitamin E ( ⁇ -tocopherol)
  • vitamin E-acetate O-acety
  • Table 2 The results presented in Table 2 are those of liquid formulations that have been stored at ambient conditions up till 7 weeks.
  • the GC-MS and GC results presented in tables 1 and 2 respectively depict a measure of stability of the unsaturated soap (detection of hexanal, heptanal and octanal) and of the iron catalyst in the formulation (pyridin-carboxyldehyde only for the results presented in Table 1) .
  • Bottles tests were done (25 mL solution) , each bottle containing two tomato stained cloths (4x4 cm) .
  • the cloths were washed for 30 min at 40 °C .
  • the dosage of formulation A was 5 g/1.
  • the water hardness used was 24 °FH.
  • the difference in ⁇ R between both reflectance values gives a measure of the bleaching performance of the system on the stain, i.e. a higher ⁇ R value corresponds to an improved bleaching performance.
  • Table 1 Amounts of aldehydes detected by GC-MS and bleach results of the liquid detergent formulations containing catalyst and anti-oxidants. Liquids stored at 37 °C . * Liquid stored at room temperature for 6 days .
  • Table 2 Amounts of aldehydes detected by GC analysis of the liquid detergent formulations containing catalyst and anti-oxidants. Liquids stored at room temperature
  • Composition formulation A A:

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PCT/EP2002/002768 2001-03-14 2002-03-11 Bleaching catalysts with unsaturated surfactant and antioxidant WO2002072747A1 (en)

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BRPI0206044-2B1A BR0206044B1 (pt) 2001-03-14 2002-03-11 Composição alvejante
EP02732479A EP1368451B1 (en) 2001-03-14 2002-03-11 Bleaching catalysts with unsaturated surfactant and antioxidant
AU2002304851A AU2002304851B2 (en) 2001-03-14 2002-03-11 Bleaching catalysts with unsaturated surfactant and antioxidant
CA2431006A CA2431006C (en) 2001-03-14 2002-03-11 Bleaching catalysts with unsaturated surfactant and antioxidant
DE60220381T DE60220381T2 (de) 2001-03-14 2002-03-11 Bleichkatalysatoren mit ungesättigtem tensid und antioxidant

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GBGB0106285.0A GB0106285D0 (en) 2001-03-14 2001-03-14 Air bleaching catalysts with moderating agent

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EP1368451B1 (en) 2007-05-30
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GB0106285D0 (en) 2001-05-02
US20030054967A1 (en) 2003-03-20
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